ArticlePediatric nephrology (Berlin, Germany)2010
Management of regional citrate anticoagulation in pediatric high-flux dialysis: activated coagulation time versus post-filter ionized calcium.
Article in Pediatric nephrology (Berlin, Germany), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 16 citations in OpenAlex.
- Kidney replacement therapy in pediatric patients on mechanical circulatory support: challenges for the pediatric nephrologist.Pediatric nephrology (Berlin, Germany) · 2021Review
- Fully printed prothrombin time sensor for point-of-care testing.Biosensors & bioelectronics · 2021Article
- Regional citrate anticoagulation in hemodialysis: an observational study of safety, efficacy, and effect on calcium balance during routine care.Canadian journal of kidney health and disease · 2016Article
- Citrate anticoagulation for continuous renal replacement therapy in small children.Pediatric nephrology (Berlin, Germany) · 2014Article
- Alternatives to standard unfractionated heparin for pediatric hemodialysis treatments.Pediatric nephrology (Berlin, Germany) · 2012Review
- Continuous renal replacement therapy in neonates weighing less than 3 kg.Korean journal of pediatrics · 2012Article
- Regional citrate anticoagulation--a safe and effective procedure in pediatric apheresis therapy.Pediatric nephrology (Berlin, Germany) · 2011Article
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Authors and funding
5 authors at 1 institution in 1 country.
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Abstract
Recent years has seen an increasing use of regional citrate anticoagulation in pediatric dialysis. Several approaches have been described for monitoring anticoagulation in the extracorporeal circuit, such as serum citrate levels, post-filter ionized calcium (iCa), and activated coagulation time (ACT). However, no standard recommendations have yet been established for applying any of these parameters, especially for iCa. The objective of this retrospective analysis was to establish adequate coagulation management using post-filter iCa values. Normal values for ACTester-based ACT were established using a group of 64 children who were divided into two subgroups, with one subgroup comprising children without chronic kidney disease or coagulation disorder (age 1.2-17.5 years, median 9.7 years) and one consisting of 32 uremic patients (age 0.6-17.5 years, median 13.7 years). In a second group of 13 patients (aged 7-17 years), all of whom were undergoing high-flux dialysis (HD) with regional citrate anticoagulation (RCA), we assessed 73 post-filter blood samples for ionized calcium and ACT. A receiver operating characteristic graph was used to identify the iCa threshold needed to achieve adequate anticoagulation. Normal values for ACT were 90 s [2 standard deviations (SD) 72-109] in healthy children and 94 s (2 SD 75-113) in the uremic children. There was no statistically significant difference between the groups. In the children undergoing HD with RCA, the post-filter iCa level correlated with ACT (r = -0.94, p < 0.001). A post-filter iCa level of < or = 0.30 mmol/l reliably predicted an ACT >120 s. Our citrate protocol [citrate 3% rate (ml/h) approximately blood flow rate (ml/min) x 2] meets the established criteria with a high sensitivity. Based on these results, we conclude that the post-filter iCa level can be reliably used for the management of extracorporeal anticoagulation with citrate in pediatric HD. We recommend the application of our citrate prescription protocol in the setting of pediatric intermittent hemodialysis.
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